Abstract

Precise regulation of gene expression during biological processes, including development, is often achieved by combinatorial action of multiple transcription factors. The mechanisms by which these factors collaborate are largely not known. We have shown previously that Isl1, a Lim-Homeodomain transcription factor, and Pou4f2, a class IV POU domain transcription factor, co-regulate a set of genes required for retinal ganglion cell (RGC) differentiation. Here we further explore how these two factors interact to precisely regulate gene expression during RGC development. By GST pulldown assays, co-immunoprecipitation, and electrophoretic mobility shift assays, we show that Isl1 and Pou4f2 form a complex in vitro and in vivo, and identify the domains within these two proteins that are responsible for this interaction. By luciferase assay, in situ hybridization, and RNA-seq, we further demonstrate that the two factors contribute quantitatively to gene expression in the developing RGCs. Although each factor alone can activate gene expression, both factors are required to achieve optimal expression levels. Finally, we discover that Isl1 and Pou4f2 can interact with other POU and Lim-Homeodomain factors respectively, indicating the interactions between these two classes of transcription factors are prevalent in development and other biological processes.

Highlights

  • Retinal ganglion cells (RGCs) are projection neurons in the vertebrate retina whose axons form the optic nerve and project to the brain [1,2]

  • Isl1 and Pou4f2 interact physically To explore the mechanism of Isl1/Pou4f2 collaboration, we first used Glutathione s-transferase (GST) pull-down assay to investigate whether these two proteins can directly interact with each other

  • Isl1 has been reported to interact with many proteins, and in most cases, the domains involved in proteinprotein interaction are the two Lim domains [37,40]

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Summary

Introduction

Retinal ganglion cells (RGCs) are projection neurons in the vertebrate retina whose axons form the optic nerve and project to the brain [1,2]. RGCs emerge from the mutipotent retinal progenitors cells [3]. RGC development is subject to control by a hierarchical gene regulatory network in which key transcription factors occupy key nodes of the network [5,6]. Math, Isl, and Pou4f2, in the network play essential roles in RGC development. Math is essential for RGC formation by rendering retinal progenitor cells competent for the RGC fate, and Isl and Pou4f2 ( known as Brn3b), not required for RGC birth, are downstream of Math and required for their differentiation [5,7,8,9,10,11,12,13]

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